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Most HIV-infected individuals develop antibodies to the gp120 and gp41 components of the viral spike; however, only a fraction of these individuals mount a broadly neutralizing serum response against HIV. We have cloned anti-HIV antibodies from the memory B-cell compartment of six individuals with variable viral loads and high titers of broadly neutralizing antibodies. Here, we report on the features of the anti-gp41 response in these patients. Competition experiments with previously characterized antibodies targeting defined epitopes on the gp41 ectodomain showed antibodies directed against the “immunodominant region” (cluster I), the carboxy-terminal heptad repeat (cluster II), and the membrane-proximal external region (cluster IV). On the other hand, antibodies directed against the amino-terminal part of the molecule, including the fusion peptide, polar region, and the N-terminal heptad repeat, were not detected. When all patients' data were combined, unique B-cell clones targeting cluster I, II, and IV accounted for 32%, 49%, and 53% of all anti-gp41-reactive B cells, respectively; therefore, no single region was truly immunodominant. Finally, although we found no new neutralizing epitopes or HIV-1-neutralizing activity by any of the gp41 antibodies at concentrations of up to 50 μg/ml, high concentrations of 7 out of 15 anti-cluster I antibodies neutralized tier 2 viruses.
The trimeric envelope spike of the human immunodeficiency virus (HIV) consists of three heterodimers of the transmembrane glycoprotein (gp41) and the surface glycoprotein (gp120) (59). Whereas gp120 carries the CD4 and chemokine receptor binding sites, gp41 is crucial for fusion between the viral particle and the cell membrane (Fig. (Fig.1a).1a). The glycine-rich fusion peptide, located at the amino-terminal region of gp41, is normally covered by gp120 but is transiently exposed for interaction with the target cell membrane when gp120 binds to its receptors (14). The fusion peptide is followed by a serine/threonine-rich polar region and heptad repeats, which form leucine zippers that mediate assembly of the coiled-coiled form of gp41 in response to gp120 engagement (8, 22, 24, 52). Finally, the membrane-proximal external region (MPER) also plays a role in virus-host membrane fusion (38); however, the mechanism by which it enhances fusion is not known.
Some regions of gp41 are accessible to antibodies on the native gp140 trimer; however, others are exposed to the immune system only after gp120 shedding (40). In addition, otherwise cryptic gp41 epitopes are uncovered during viral fusion with the cell membrane (13). Consistent with gp41 exposure to the immune system, serologic studies of infected individuals indicate that there is a strong humoral response to gp41 during HIV infection (35) which precedes the response against gp120 (26).
Antibodies to gp41 have been isolated from phage display libraries, as have Epstein-Barr virus (EBV) immortalized B cells from infected individuals (4, 53). Some of these anti-gp41 antibodies can neutralize HIV infection in vitro and interfere with the virus in vivo (4, 6, 50). However, there has yet to be a systematic study of the anti-gp41 memory B-cell response of individuals with high titers of broadly neutralizing anti-HIV antibodies.
In order to document the nature of the anti-gp41 antibody response in HIV-infected individuals with high titers of broadly neutralizing antibodies, we studied 131 such antibodies, accounting for 47 unique B-cell clones, which we obtained from the memory B-cell compartments of six patients with low-to-moderate HIV viral titers (43). Each unique clone was composed of up to 15 clonal members that were either identical or related by somatic mutation. The largest number of unique B-cell clones, 53%, was directed to a conformational epitope which neighbors the MPER (cluster IV), 49% were directed to the carboxy-terminal heptad repeat (cluster II), and 32% were directed to the previously identified “immunodominant region” (cluster I), of which 60% recognize a linear peptide (amino acids 579 to 604). Furthermore, B cells producing antibodies to this region comprise large expanded clones. In total, 57 out of the 131 anti-gp41 and 502 anti-gp140 antibodies cloned were directed to cluster I, some of which show tier 2 virus-neutralizing activity at high antibody concentrations.
The HIV-1-infected patients were part of the Elite Controller Study of the Partners Aids Research Center (patients 2, 3, and 5) and clinical protocols at the Aaron Diamond Research Center (patient 1) and the National Institute of Allergy and Infectious Diseases (patients 4 and 6). The uninfected volunteer (healthy control [HC]) was recruited at the Rockefeller University. All work with human samples was performed in accordance with approved Institutional Review Board protocols (43).
Biotinylated HIV-1 gp41 (Prospec) contained the full-length extracellular domain of strain IIIB (amino acids [aa] 513 to 674). To coat streptavidin-magnetic beads (Dynal M-280 Streptavidin; Invitrogen) with HIV-1 gp41, 10 mg of beads was incubated with 100 μg of protein at room temperature for 45 min on a shaking platform. IgG was purified, dialyzed against Dulbecco's phosphate-buffered saline (DPBS; Gibco) and incubated with the coated and washed beads for 1 h at a ratio of 10 mg of coated beads per 10 mg of IgG. Following magnetic bead removal, the IgG was adsorbed five more times to ensure maximal adsorption. Beads containing the gp41-positive IgG fraction were washed with DPBS (Gibco) three times before specific antibody elution with 0.1 M glycine buffer, pH 3, into 1 M Tris-HCl buffer, pH 8.
Specificity of HIV-1 gp41 binding antibodies was determined by competition enzyme-linked immunosorbent assays (ELISAs). Cloned anti-gp41 antibodies were biotinylated (EZ-Link Micro Sulfo-NHS-Biotinylation Kit; Pierce), and their specificities were initially determined by competition with previously characterized anti-gp41 cluster antibodies (Fig. (Fig.1b):1b): D61 to cluster I amino acids 597 to 613 (12); D40, D17, and D50 to cluster II amino acids 642 to 665 (12); 4E10 and 2F5 to cluster III amino acids 662 to 678 (60); T3 to cluster IV amino acids 641 to 68 (12); and T30 to cluster VI amino acids 611 to 640 (12). The biotinylated antibodies 4E10 and 2F5 (cluster II), 2-378 and 2-55 (cluster I; the first number in designations of this type indicate the patient), 1-763 (cluster II and IV), and 3-255 (cluster IV) were then used in direct competition experiments to determine the properties of the remaining anti-gp41 antibodies.
ELISAs were performed with high-binding capacity ELISA plates (Costar) coated with 50 μl of gp41 (ectodomain aa 541 to 682; strain HxB2) (Acris, Herford) at 5 μg/ml in phosphate-buffered saline (PBS) overnight at room temperature. This protein preparation contains three major immunospecific bands migrating between 20 and 30 kDa, minor bands between 20 and 30 kDa, bands at 14 and 7 kDa, and an aggregation smear at 35 kDa and greater, as indicated by the manufacturer (Acris, Herford, Germany) (see Fig. Fig.6a).6a). Plates were washed three times with 200 μl of ultrapure water per well and incubated with 100 μl of blocking buffer (2 mM EDTA and 0.05% Tween-20 in PBS) for 30 min at room temperature and washed again. Biotinylated antibodies (0.8 μg/ml) were mixed with 4-fold serial dilutions of the competing antibodies starting at 10 μg/ml before they were applied to the coated ELISA plate. After 2 h of incubation at room temperature, plates were washed as described above. Bound biotinylated antibodies were detected with streptavidin-horseradish peroxidase (HRP) conjugate (AbD). The complex was detected with an HRP substrate kit (Bio-Rad) and measured at 405 nm to calculate the half-maximal (50%) inhibitory concentration (IC50) of the unbiotinylated antibodies.
Peptide ELISAs were performed as previously described (32). Briefly, ELISA plates (Costar) were coated with 50 μl of the peptide recognized by 2F5 (SQNQQEKNEQELLALDKWAS; underlining refers to the minimal epitope) or 4E10 (LWNWFDITKWLWYIKIFIMI) at 5 μg/ml in PBS and incubated overnight at room temperature. After plates were washed three times with PBS-0.1% Tween 20 (PBST), wells were blocked with PBS-1% Tween 20-5% sucrose-3% milk powder for 1 h at room temperature. Serial dilutions of human IgG (starting at 100 μg/ml in PBST-1% bovine serum albumin [BSA]) were added, and samples were incubated for 1 h at room temperature and visualized with peroxidase-conjugated affinity-purified goat anti-human IgG (Jackson) using an HRP substrate kit (Bio-Rad). Controls were HC IgG, polyclonal HIV-1 immune globulin (HIV IG), 2F5, and 4E10 (Polymun Scientific, Austria), each of which was included in every experiment.
To remove N-linked glycans, 50 μg of gp41 was treated with peptide N-glycosidase F (PNGase F; New England Biolabs) in 50 mM sodium phosphate at 37°C under nondenaturing conditions for 12 h. Deglycosylation was confirmed by band shift on an SDS-polyacrylamide (PA) gel with Coomassie blue staining and by lectin precipitation (agarose-bound Lens culinaris agglutinin; Vector Laboratories, Burlingame, CA), followed by elution with 0.5 M methyl α-d-mannopyranoside (Sigma) of the glycosylated, but not deglycosylated, gp41.
Neutralization assays were performed as described previously (27, 29). Briefly, neutralization was detected as a reduction in firefly luciferase reporter gene expression after infection of TZM-bl cells with HIV-1 envelope glycoprotein (Env) pseudovirus variants. Murine leukemia virus was used as a negative control to rule out nonspecific toxicity by the antibodies.
We cloned antibodies to gp140 from the memory B-cell compartment of six patients with variable viral loads and high titers of broadly neutralizing antibodies by staining cells with artificially trimerized gp140 (43). Although we did not find any monoclonal antibodies with broad neutralizing activity among the 502 cloned IgG antibodies to gp140, combinations of antibodies showed a breadth of neutralizing activity at high concentrations (43, 54). To determine whether antibodies to gp41 might contribute to the neutralizing activity in the serum of these patients, we adsorbed purified serum IgG on gp41. The depleted and gp41 binding fractions were tested for gp41 binding by ELISA, as well as for neutralizing activity on a previously described panel of tier 1 and tier 2 viruses (23). Anti-gp41 binding antibodies were efficiently depleted and recovered after adsorption on gp41 (Fig. (Fig.2a2a).
Unfractionated IgG neutralized HIV at concentrations ranging from 2 μg/ml up to 1,138 μg/ml (Table (Table1).1). For two of three patients studied, removal of the anti-gp41 binding antibodies resulted in a 2- to 3-fold increase in neutralizing potency; however, patient 3 showed a smaller increase and, for some viruses, a decrease in neutralizing activity after the removal of gp41 binding antibodies (Fig. (Fig.3).3). Consistent with the observation that anti-gp41 antibody depletion did little to alter the overall neutralizing activity, the purified anti-gp41 antibodies were significantly less active than unfractionated IgG in neutralization assays. We conclude that the anti-gp41 antibodies did not significantly contribute to the neutralizing activity of the patient sera studied. These findings are consistent with the observation that broad neutralizing activity in serum is not usually due to anti-gp41 antibodies (35, 48), with the exception of rare anti-MPER antibodies (18). However, since there are several distinct conformational states of gp41 during viral entry, including the prefusion, prehairpin intermediate, and postfusion conformations, we cannot rule out the possibility that not all anti-gp41 antibodies have been adsorbed and depleted by the soluble form of the protein used here.
To characterize the epitopes recognized by the cloned anti-gp41 memory antibodies in the six patients with variable viral loads and high titers of broadly neutralizing serum antibodies, we performed competition ELISAs with well-characterized anti-gp41 antibodies (12, 43). We examined all of the previously reported unique anti-gp41 antibodies cloned from memory B cells (43). The following anti-gp41 antibodies were used as standards (Fig. (Fig.1b)1b) (11, 12, 57): D61, which recognizes an amino-terminal determinant, corresponding to the immunodominant region, and spans amino acids 597 to 613 (cluster I; LAI strain) (12); D40, D17, and D50, which bind to a region (cluster II) that includes amino acids 642 to 665 located at the amino terminus of the MPER; 4E10 and 2F5, which bind to separate but adjacent peptides in the MPER that span amino acids 662 to 678 (cluster III); T3, which binds a conformational epitope neighboring the MPER and spans amino acids 641 to 683 (cluster IV); and T30, which binds the carboxy terminus of cluster I, amino acids 611 to 640 (cluster VI).
Despite some degradation in the gp41 protein preparation (see Fig. Fig.6a),6a), anti-cluster I, -cluster II, -cluster IV, and -cluster VI antibodies accounted for all of the anti-gp41 binding by the monoclonal antibodies isolated from patients with high titers of broadly neutralizing antibodies (Fig. (Fig.44 and and55 and Table Table2).2). However, the distribution of unique, nonclonal antibodies varied between patients. For example, cluster I antibodies were most abundant in patient 2, and cluster II antibodies were most abundant in patient 3. When combined, the largest number of unique B-cell clones was directed to cluster IV (53%), followed by cluster II antibodies (49%) and cluster I antibodies (32%) (the sum shown in Table Table2,2, 134%, results from antibodies that bind to two clusters). Although none of the antibodies tested interfered with the binding of the MPER-specific cluster III antibodies 4E10 and 2F5, antibodies to clusters II and IV, which flank this region, were common; therefore, this region of the molecule is accessible to the immune system in vivo. Indeed, each of the patients showed several antibodies that inhibited binding by both anti-cluster II and -cluster IV antibodies but not by cluster III antibodies, despite the proximity of these epitopes. The most likely explanation for the overlap between cluster II and cluster IV antibodies is the fact that cluster II antibodies recognize an epitope that is contained within the larger, conformationally dependent cluster IV epitope (12).
Each of the unique antibodies tested was a member of a clone of antibodies ranging in size from 1 to 15 members. Together, 47 unique B-cell clones were expanded to account for a total of 131 independent antibodies. Within cluster I, antibody clones against linear (amino acids 579 to 604 ) and nonlinear epitopes were highly expanded in all of the patients except patient 3, who showed no antibodies to this region. Anti-cluster I antibodies comprised 15 different clonal families, with a total of 57 members. When the detected antibodies were combined, 32% of all unique anti-gp41 B-cell clones and 44% of all the anti-gp41 antibodies we obtained targeted this region. In contrast, antibodies to clusters II and IV comprised 49% and 53% of all unique anti-gp41 B-cell clones, respectively, and 40% each of all the anti-gp41 antibodies (the sum is greater than 100% because some antibodies appear to bind to two epitopes) (Table (Table2).2). Thus, antibodies to cluster I of gp41 are highly represented but not immunodominant in the memory B-cell compartment of the patients studied (53).
To confirm the absence of MPER-directed 2F5- and 4E10-like antibodies in the patients' sera, we performed competition ELISAs between affinity-purified anti-gp41 patient IgG and biotinylated 4E10 and 2F5. Controls included HIV IG, which did not inhibit 4E10 or 2F5 binding, as well as unbiotinylated 4E10 and 2F5 and IgG from noninfected individuals. Consistent with the results obtained with the monoclonal antibodies, the patients' affinity-purified anti-gp41 IgG did not block the binding of 4E10 or 2F5 to gp41 (Fig. (Fig.2b).2b). However, as expected, the same affinity-purified fraction (shown for patient 1) blocked the binding of cluster I antibodies (2-55 and 2-378) (Fig. (Fig.2c).2c). To increase the sensitivity of the assay, we performed ELISAs with anti-2F5 and -4E10 peptides (Fig. (Fig.2d).2d). HIV IG bound to the 2F5 peptide at very high concentrations (>25 μg/ml), indicating that only rare or low-affinity antibodies to this peptide exist in HIV IG, and we found no binding to either peptide by our patients' IgG. We conclude that none of the patients studied produced significant titers of antibodies against the 2F5- and 4E10-like MPER epitopes.
To determine whether binding of any of the anti-gp41 antibodies was carbohydrate dependent, we deglycosylated gp41 with PNGase F to remove N-linked glycans and repeated the ELISAs. Deglycosylation was confirmed by a shift in mobility on denaturing polyacrylamide gels (Fig. (Fig.6a)6a) and by lectin precipitation (Fig. (Fig.6b).6b). Glycosylated gp41 bound to Lens culinaris lectin-Sepharose, whereas deglycosylated gp41 did not (Fig. (Fig.6b).6b). We found one monoclonal anti-gp41 antibody (4-157) whose binding was carbohydrate dependent (Fig. (Fig.6c).6c). This antibody was mapped to cluster I by competition experiments, but did not bind to the immunodominant peptide (amino acids 579 to 604).
None of the anti-gp41 antibodies showed neutralizing activity at concentrations up to 50 μg/ml (43). To determine whether any of the 47 anti-gp41 antibodies showed neutralizing activity at higher concentrations, we performed in vitro neutralization assays with antibody concentrations of up to 2,380 μg/ml on two tier 2, clade B, Env-pseudotyped viruses from primary isolates (TRO.11 and RHPA4259.7). We found that 7 out of 15 cluster I antibodies were able to neutralize TRO.11 at high concentrations ranging from 433 to 1,712 μg/ml (IC50). Among all other antibodies, only one antibody against cluster IV showed neutralization at 1,276 μg/ml (Table (Table3).3). We conclude that, among anti-gp41 antibodies, those directed to cluster I show neutralizing activity but only at very high concentrations.
gp41 is highly immunogenic and elicits antibodies in almost all HIV-infected individuals, with titers that can exceed 1:106 (2, 53). These titers are 25- to 625-fold higher than anti-gp120 titers (35). In addition, gp41 differs from gp120 in that all regions of the protein appear to be targeted by the human antibody response (35).
Serologic examination of 23 randomly selected HIV-1-positive individuals showed that the fusion peptide and the polar region induce low-to-medium serum antibody titers (35). In contrast, high serum antibody titers (up to 1:7 × 105) were documented against the N- and C-terminal heptad repeats (35), the membrane-proximal region (35), and the cluster I region (53). The latter was identified as immunodominant by the observation that 53 out of 53 HIV-positive patients' sera tested showed reactivity to a synthetic 12-mer peptide from this region (LGLWGCSGKLIC) (15, 16). Consistent with this peptide's immunogenicity, injection of the peptide coupled to keyhole limpet hemocyanin into rabbits resulted in serum antibody titers of 1:1 × 106 (15). Although antibodies to the antigens that are membrane proximal are also present in most patients' sera, these do not appear to resemble the broadly neutralizing 2F5- and 4E10-like antibodies (18, 56). Instead, the anti-MPER antibodies that were commonly found among patients appear to be directed to a peptide partially overlapping the 2F5 and 4E10 epitope (amino acids 665 to 683) (35). Similarly, gp41-immunized rabbits produced antibodies to cluster I but failed to produce anti-MPER antibodies (58).
In contrast to the serologic studies described above, which were performed on immunized rabbits and randomly selected HIV-1-infected individuals, our patients were selected for broad neutralizing antibody responses, relatively low viral titers, and moderate CD4+ T-cell counts (43). In addition, the B cells from which our antibodies were cloned were selected for their binding to soluble trimeric gp140 (54), which is recognized by most anti-gp41 antibodies, including those binding to the MPER, the C-terminal heptad repeat, cluster I, and the fusion peptide polar region (antibody 5F3) (6). However, antibody D3 mapped to cluster V, which includes the fusion peptide, the polar region, and the N-terminal heptad repeat, does not recognize the synthetic trimer (data not shown); therefore, antibodies with this type of reactivity to gp41 would not be detected in our analysis.
We found that 47 unique clones of anti-gp41 antibodies were variably expanded, with each containing 1 to 15 members, for a total of 131 independently cloned antibodies. All of these antibodies could be assigned to clusters I, II, IV, and VI, but none recognized the fusion peptide, the polar region, or the N-terminal heptad repeat or the MPER peptide. This finding is consistent with both the absence of antibodies to the MPER peptide in the patient serum and the inability of a control anti-cluster V antibody to bind to the artificial gp140 trimer. Unique antibodies reacting with cluster I, the immunodominant region, were not predominant in the collection; they represented only 32% of all the unique B-cell clones. Instead, a conformational epitope neighboring the MPER (cluster IV) was the dominant immunogen. However, anti-cluster I clones were disproportionately expanded, accounting for 44% of all anti-gp41 antibodies when all of the distinct clonal family members were considered. Among the 15 unique clones of anti-cluster I antibodies, 9 recognized the linear peptide, and 6 were against conformational determinants in this region. Similarly, 5 out of 10 antibodies produced from seven seropositive patients by EBV immortalization were directed to cluster I, and of these, 4 were directed to the linear peptide (53). In contrast, phage display antibody libraries that were constructed from patients and that were selected on recombinant gp41 showed a much lower frequency of cluster I binders (5 out of 25) (4). However, antibody cloning by phage display is biased by multiple rounds of selection and amplification; in addition, the process may not reflect the native antibody repertoire because heavy and light chains are paired randomly, potentially creating novel combining sites. Thus, the frequency of specific antibodies estimated by this method may not be an accurate reflection of the antibodies found in a patient's B-cell repertoire. We conclude that in patients with high titers of broadly neutralizing HIV antibodies and variable viral loads, anti-cluster I antibodies account for 32% of all unique B-cell clones; these are preferentially expanded to account for 44% of all anti-gp41 antibodies, a significant fraction of which are directed to the linear peptide comprised of amino acids 579 to 604. The gp41 antibodies found in the patients studied might result from B-cell stimulation by the intact virion or by nonfunctional membrane-associated gp41 on the surface of infected cells or even damaged virions (7, 19, 31).
Our studies reveal several previously unappreciated epitopes on gp41. For example, four antibodies cloned from the memory B cells were inhibited by monoclonal antibodies directed to both cluster I and IV but not by antibodies to cluster VI, which is between the two. Inhibition by anti-cluster I and -cluster IV but not anti-cluster VI suggests that the former two are closely opposed to each other in the trimer, either in cis or in trans between two different gp41 molecules in the trimer.
In addition to conformational epitopes within cluster I, we found a novel carbohydrate-dependent epitope in the same region of gp41. This region contains three well-conserved, predicted glycosylation sites (21). Like 2G12, which recognizes a carbohydrate-dependent epitope on gp120 (42), gp41 binding by antibody 4-157 is sensitive to deglycosylation, which thereby establishes that the cluster I region of gp41 is indeed glycosylated (21).
Among the 345 amino acid residues in gp41, one-third show up to 90% conservation among HIV-1 group M isolates (20). These include highly conserved residues critical for the formation of the coiled-coil gp41 pocket (28), for gp120-gp41 interactions (55), and for envelope biosynthesis (45). These critical residues are found primarily in the heptad repeats and the cluster I region. Indeed, mouse anti-cluster I antibodies exhibit extensive cross-reactivity with primary envelope proteins from divergent HIV-1 clades, indicating the presence of a highly conserved secondary antigenic structure in the cluster I loop region (12). Given the importance of these regions in the function of the viral spike and their relatively high level of conservation, these might be important targets for neutralizing antibodies if they were accessible either on the virion or as membrane-associated gp41 postfusion on the surface of infected cells. Consistent with this idea, the IgG fraction of serum from rabbits immunized with gp41 neutralized 52% of 21 HIV primary isolates in a peripheral blood mononuclear cell (PBMC)-based assay, with IC50s lower than 50 μg/ml (58). Finally, several groups of investigators have recently shown that a small fraction of HIV-infected patients develops anti-gp41 neutralizing antibody responses, mainly due to anti-MPER antibodies (3, 39, 47).
Despite the serologic data noted above, there are only a few neutralizing monoclonal anti-gp41 antibodies. D5 is a phage-derived antibody obtained from a naïve single-chain variable-fragment (scFv) library that inhibits the assembly of fusion intermediates in vitro by binding to the N-terminal heptad repeat (27). Antibody m44, another phage-derived antibody, recognizes a conformational epitope implicated in the binding of the C-terminal heptad repeat (57). Less is known about how this antibody inhibits infection, but the mechanism may be related to the one used by D5 since both target the heptad repeats that form six-helix coiled-coiled fusion intermediates in vitro. Clone 3 is specific for the immunodominant region and shows neutralizing activity against a diverse group of laboratory-adapted HIV-1 strains (10, 51). This antibody was produced by EBV-transformed PBMCs from an asymptomatic HIV-1-positive donor (10). Other antibodies against this region show complement-mediated infection-enhancing activity in vitro (36, 37).
Finally, there are three broadly neutralizing antibodies directed to the membrane-proximal external region: 2F5 (33, 49), 4E10, and Z13 (60). Such antibodies are rare (3) and were detected only in the sera of 3 out of 156 chronically HIV-1-infected individuals (17). The poor immunogenicity of this region may be attributed to its lack of exposure on the surface of the native virus (9, 34, 41, 44; reviewed in reference 30). The neutralizing activity of these antibodies appears to be dependent on binding to both the MPER and to the viral membrane (25). It has been proposed that antibody binding to the viral membrane serves to concentrate the antibody in the region of the MPER, thereby favoring its interaction with this poorly exposed antigenic epitope (1). Consistent with the idea that lipid binding may be important in the function of the anti-MPER antibodies, liposomes containing MPER peptide induced multispecific antibodies that simultaneously recognize the lipid and the MPER antigen; they also neutralized HIV SF162 in a PBMC-based neutralization assay (25).
We found that none of the gp41 antibodies cloned from the memory B cells of the six individuals studied were able to neutralize HIV at concentrations of up to 50 μg/ml (43). Surprisingly, 7 out of 15 antibodies to cluster I neutralize one of two tested tier 2 viruses at high concentrations. Although it is unlikely that an individual anti-cluster I antibody would have a biological effect, large numbers of gp41 antibodies might enhance neutralizing activity due to additive or even synergistic neutralizing effects (43). Antibody binding to the cluster I hinge region between the heptad repeats might interfere with the formation of the prehairpin fusion intermediate by steric hindrance (27). Why such high concentrations of cluster I antibodies are necessary for neutralization remains unclear (5); one possibility is that this region is poorly accessible to antibodies binding the intact virion.
We thank Henry Zebrosky, Rockefeller Proteomics Resource Center, for the production of gp41 peptides. The following reagents were obtained through the AIDS Research and Reference Reagent Program, Division of AIDS, NIAID, NIH: HIV IG from NABI and NHLBI and HIV-1 gp41 monoclonal antibody (5F3) from Hermann Katinger.
The work was supported by NIH grant 1 P01 AI08677-01 and a grant from the International AIDS Vaccine Initiative. M.C.N. is a Howard Hughes Medical Institute investigator.
Published ahead of print on 10 March 2010.